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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT04082117
Other study ID # 2016-1219
Secondary ID
Status Active, not recruiting
Phase N/A
First received
Last updated
Start date May 12, 2017
Est. completion date May 2024

Study information

Verified date September 2023
Source University of Illinois at Chicago
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

A feasibility study incorporating an educational intervention with cancer genetic risk assessment (CGRA) in the UI Health mammography center


Description:

African American (AA) women with a family history of breast cancer who are eligible for genetic counseling and express an interest in participating in the study will be consented and complete a brief survey before and after viewing an educational video on genetic counseling. Survey questions will be read to each participant. The questions capture data on the following constructs regarding genetic counseling: knowledge, attitudes, normative beliefs, motivation, perceived social norms, intention, efficacy beliefs, skills, environmental constraints and opinions on the video. The research team will conduct a review of the UI Health Electronic Medical Record (EMR) 3-6 months after study enrollment to determine if the participant attended a genetic counseling session.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 960
Est. completion date May 2024
Est. primary completion date May 2024
Accepts healthy volunteers No
Gender Female
Age group 25 Years to 69 Years
Eligibility Inclusion Criteria: - African American female age 25-69 years - Presenting for mammogram at UI Health mammography clinic - No prior history of breast cancer - Completed cancer genetic risk assessment (CGRA) in UI Health mammography center - Recommended for genetic counseling based on CGRA performed at the time of the mammogram. Exclusion Criteria: - Unable to complete the informed consent and survey in English - Previously had genetic counseling for hereditary breast cancer risk - Prisoners

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Educational video
Educational genetic counseling video

Locations

Country Name City State
United States University of Illinois Chicago Illinois
United States University of Illinois Health System Chicago Illinois

Sponsors (1)

Lead Sponsor Collaborator
University of Illinois at Chicago

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Knowledge and intentions regarding genetic counseling Change in knowledge of genetic counseling and intention to engage in genetic counseling following viewing of educational video based on response to survey designed by study investigators. 1 hour
Secondary Attendance at genetic counseling appointment Rate that study participants attend a genetic counseling appointment within 3 months of viewing educational video 3 months
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